Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population

BACKGROUND: Genetics clearly plays a major role in the etiology of autism spectrum disorders (ASDs), but studies to date are only beginning to characterize the causal genetic variants responsible. Until recently, studies using multiple extended multi-generation families to identify ASD risk genes ha...

Descripción completa

Detalles Bibliográficos
Autores principales: Matsunami, Nori, Hensel, Charles H, Baird, Lisa, Stevens, Jeff, Otterud, Brith, Leppert, Tami, Varvil, Tena, Hadley, Dexter, Glessner, Joseph T, Pellegrino, Renata, Kim, Cecilia, Thomas, Kelly, Wang, Fengxiang, Otieno, Frederick G, Ho, Karen, Christensen, Gerald B, Li, Dongying, Prekeris, Rytis, Lambert, Christophe G, Hakonarson, Hakon, Leppert, Mark F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4098669/
https://www.ncbi.nlm.nih.gov/pubmed/24467814
http://dx.doi.org/10.1186/2040-2392-5-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4098669/
https://www.ncbi.nlm.nih.gov/pubmed/24467814
http://dx.doi.org/10.1186/2040-2392-5-5

Ejemplares similares